Nicolas Lacoste

CNRS UMR 5261, INSERM U1315, Faculté De Médecine Lyon Est
Lyon, France

Last Updated: 09/26/2026

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Found 9 publications

Homozygous COQ9 mutation: a new cause of potentially treatable hereditary spastic paraplegia.

Homozygous COQ9 mutation: a new cause of potentially treatable hereditary spastic paraplegia.

Journal: European journal of human genetics : EJHG

Published: January 29, 2025

H2A.Z is involved in premature aging and DSB repair initiation in muscle fibers.

H2A.Z is involved in premature aging and DSB repair initiation in muscle fibers.

Journal: Nucleic acids research

Published: April 04, 2023

Reply: Biallelic variants in the COQ7 gene cause distal hereditary motor neuropathy in two Chinese families.

Reply: Biallelic variants in the COQ7 gene cause distal hereditary motor neuropathy in two Chinese families.

Journal: Brain : a journal of neurology

Published: January 03, 2023

Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy-Case Report.

Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy-Case Report.

Journal: Genes

Published: October 26, 2022

LSD1 controls a nuclear checkpoint in Wnt/β-Catenin signaling to regulate muscle stem cell self-renewal.

LSD1 controls a nuclear checkpoint in Wnt/β-Catenin signaling to regulate muscle stem cell self-renewal.

Journal: Nucleic acids research

Published: September 13, 2022

Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy.

Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy.

Journal: Brain : a journal of neurology

Published: July 18, 2022

Expanding the phenotypic variability of MORC2 gene mutations: From Charcot-Marie-Tooth disease to late-onset pure motor neuropathy.

Expanding the phenotypic variability of MORC2 gene mutations: From Charcot-Marie-Tooth disease to late-onset pure motor neuropathy.

Journal: Human mutation

Published: February 14, 2022

Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons.

Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons.

Journal: Acta neuropathologica

Published: February 01, 2022

H2A.Z is dispensable for both basal and activated transcription in post-mitotic mouse muscles.

H2A.Z is dispensable for both basal and activated transcription in post-mitotic mouse muscles.

Journal: Nucleic acids research

Published: November 14, 2019

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Last Updated: 09/26/2026